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Terminated

AVSM3 SNF, Vital Signs Monitor The monitor is intended to be used to monitor noninvasive blood pressure (NIBP), functional arterial oxygen saturation (SpO2), pulse rate (PR), temperature (Temp) for adult, pediatric and neonatal patients in all areas of a hospital and hospital-type facilities.

FDA Recall Z-2096-2021 · Posted None

Recalling FirmMediana Co., Ltd.
Recall StatusTerminated
Product CodeDXN
Date Initiated2021-05-17
Date Terminated2022-11-04
Product Quantity618

Reason for Recall

In some cases the equipment fails to power up and/or key or button unresponsive or not working.

Firm Action

The firm sent a "URGENT : Field Safety Notice(Correction)" email dated May 17, 2021 to its consignee. The email describes the product, problem and actions to be taken. The following actions were to be implemented: Implementation of action plan (1) Inventory stock a importer's hand: Mediana service engineer will update before ship to end users. (2) The products at end user's hand: Provide the modified new Software via USB memory stick and instruction for upgrading the S/W 3. Required actions for the user - INSPECT the inventory for the affected Model number, serial number(s), and date of manufacture. - IF USER HAVE affected devices Contact Customer Technical Services or Sales Representative for correction. - RETURN the enclosed acknowledgement form to Mediana USA service center. - UPGRADE THE S/W with the received s/w according to the instruction. - IF ANY Problem occurred during the upgrade Contact Customer Technical Services or Sales Representative. If you have any questions, contact QMS Representative at +82 70 7092 9945; email: [email protected]. or Sales Representative at +82 70 7092 9525; email: [email protected]. or Technical Services at 425-406-2262; email: [email protected].

Root Cause

Nonconforming Material/Component

Distribution Pattern

US Distribution to: Wisconsin only

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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